Taiwan FDA registration d831cbfee0ae2cd7cd8b752fee6c9ee9
"Xincheng" alternating decompression air mattress (unsterilized)
TW: "鑫成"交替式減壓氣墊床(未滅菌)
Taiwan·Risk Class 1·ROODINSEAT CORPORATION·Registered Jan 10, 2012 – Jan 10, 2022CancelledRegistration details
- Analysis ID
- d831cbfee0ae2cd7cd8b752fee6c9ee9
Company information
- Manufacturer
- ROODINSEAT CORPORATION
- Manufacturer Country
- Taiwan, Province of China
- Authorized Representative
- ROODINSEAT CORPORATION
Product details
- Intended Use
- Limited to the first level identification range of the Measures for the Administration of Medical Equipment "Alternating Pressure Air Mattress (J.5550)".
- Product Type (Level 1)
- J General hospital and personal use equipment
- Product Type (Level 2)
- J.5550 交替式壓力氣墊床
- Import Information
- Domestic
Dates and status
- Registration Date
- Jan 10, 2012
- Expiry Date
- Jan 10, 2022
- Cancellation Date
- Apr 12, 2024
Cancellation information
- Status
- Logged out
- Reason
- 許可證已逾有效期
About this record
Access comprehensive regulatory information for "Xincheng" alternating decompression air mattress (unsterilized) in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 1 medical device is registered under number d831cbfee0ae2cd7cd8b752fee6c9ee9 and manufactured by ROODINSEAT CORPORATION. The authorized representative in Taiwan is ROODINSEAT CORPORATION.
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